Package 0254-1010-19

Brand: diazoxide

Generic: diazoxide
NDC Package

Package Facts

Identity

Package NDC 0254-1010-19
Digits Only 0254101019
Product NDC 0254-1010
Product ID 0254-1010_ca21c9b7-669a-4f0f-afe0-0b166c13bb98
Description

1 BOTTLE, DROPPER in 1 CARTON (0254-1010-19) / 30 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2020-07-21
Brand diazoxide
Generic diazoxide
Sample Package No

Linked Drug Pages (1)

Diazoxide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ca21c9b7-669a-4f0f-afe0-0b166c13bb98", "openfda": {"upc": ["0302541010198"], "unii": ["O5CB12L4FN"], "rxcui": ["197593"], "spl_set_id": ["abe317a5-6c63-469c-89c8-9fedfe859c3d"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0254-1010-19)  / 30 mL in 1 BOTTLE, DROPPER", "package_ndc": "0254-1010-19", "marketing_start_date": "20200721"}], "brand_name": "Diazoxide", "product_id": "0254-1010_ca21c9b7-669a-4f0f-afe0-0b166c13bb98", "dosage_form": "SUSPENSION", "product_ndc": "0254-1010", "generic_name": "Diazoxide", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazoxide", "active_ingredients": [{"name": "DIAZOXIDE", "strength": "50 mg/mL"}], "application_number": "ANDA210799", "marketing_category": "ANDA", "marketing_start_date": "20200721", "listing_expiration_date": "20261231"}